HRID62692

反应详情

EQUATION

反应方程式

HRID 62692 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a solution of tert-butyl 4-((3-(2-nitro-5-(thiophen-2-yl)phenyl)ureido)methyl)piperidine-1-carboxylate (0.30 g, 0.65 mmol) in dichloromethane (15 mL) was added TFA (3 mL) at 0° C. The reaction was warmed to room temperature and stirred for 2 h. The reaction was concentrated. The crude residue was diluted with a saturated aqueous solution of sodium bicarbonate. The obtained solid was filtered, washed with water then washed with ether and pentane to afford 1-(2-nitro-5-(thiophen-2-yl)phenyl)-3-(piperidin-4-ylmethyl)urea (0.20 g, 85% yield).

WORKUP

后处理

  1. concentrationThe reaction was concentrated
  2. additionThe crude residue was diluted with a saturated aqueous solution of sodium bicarbonate
  3. filtrationThe obtained solid was filtered
  4. washwashed with water
  5. washthen washed with ether and pentane